Abstract

A bench-scale reactor is being used to conduct studies of the conversion of synthesis gas to methanol by a novel process. In previous reports, we provided evidence for a two step reaction in series: the carbonylation of methanol to methyl formate taking place in a non-equilibrium region in the vicinity of the copper chromite surface, and the hydrogenolysis of methyl formate to methanol taking place on the surface of the copper chromite. The synergism between the two catalysts enhances the rate of methanol formation. In this quarter, we tested several copper chromites (with different surface areas and stabilizing agents) on the rate of methanol synthesis. It seems likely that pore diffusion limitations control the hydrogenolysis reaction since the rate of methanol formation is proportional to the square root of the copper chromite surface area. Elemental analyses using Inductively Coupled Plasma analysis and pore size distribution analysis of copper chromite were carried out.

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